syndromic X-linked intellectual disability Pilorge type

Summary
Synonym
  • MRXSP
Definition
A syndromic X-linked intellectual disability characterized by global developmental delay with variably impaired intellectual development, speech delay, and behavioral abnormalities including autism spectrum disorder that has_material_basis_in heterozygous or hemizygous mutation in the GLRA2 gene on chromosome Xp22.
Super Class
syndromic X-linked intellectual disability
External Links
Disease Ontology
DOID:0070422
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2742 GLRA2 glycine receptor alpha 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
237213 Glra2 glycine receptor, alpha 2 subunit
Displaying 1 entry
Gene ID Gene Symbol Description Source
24397 Glra2 glycine receptor, alpha 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
172103 glc-2 Glutamate-gated chloride channel subunit beta
180086 glc-1 Glutamate-gated chloride channel alpha

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024